HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678723Generated: October 31, 2026
Triphenylphosphine → HCID 59373762, compound
https://huagongshe.com/reaction/1678723
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diamide | HCID 5353800 | — |
| Reactant | HCID 59370765 | HCID 59370765 | — |
| Reactant | HCID 67330214 | HCID 67330214 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 59373762 | HCID 59373762 | — |
Reaction Steps
Tert-butyl 3-ethyl-6-hydroxyindazole-1-carboxylate (27.9 mg) that can be produced by the method described in Reference Example 14 or the like, and a (R)-tert-butyl 5-(2-(benzyl(2-hydroxyethyl)amino)-1-(triethylsilyloxy)ethyl)-2-chlorophenyl(methylsulfonyl)carbamate-toluene solution [0.5 mL; solution prepared by dissolving (R)-tert-butyl 5-(2-(benzyl(2-hydroxyethyl)amino)-1-(triethylsilyloxy)ethyl)-2-chlorophenyl(methylsulfonyl)carbamate (1.5265 g) that can be produced by the method described in Reference Example 75 or the like in dehydrated toluene (10 mL)] were dissolved in dehydrated toluene (0.5 mL), and triphenylphosphine (54.9 mg; manufactured by Wako Pure Chemical Industries, Ltd.) and TMAD (41.4 mg; manufactured by Masuda Chemical Industries, Co., Ltd.) were added to the solution. The mixture was stirred for 3 days at room temperature. The reaction solution was purified by column chromatography (“COLUMN-B”; n-hexane:ethyl acetate=85:15→64:36), and thus the title compound (85.6 mg) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08008506B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-2140ce4f59da4b55b5427189ae094db0 |
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| Source note | uspto-grants-2011_08 |
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